Category:Tay–Sachs disease

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enfermedad de Tay-Sachs (es); Tay–Sachs-szindróma (hu); Tay Sachs-veiki (is); Tay-Sachs-en gaixotasun (eu); Болезнь Тея — Сакса (ru); Tay-Sachs-Syndrom (de); Galar Tay-Sachs (ga); بیماری تای ساکس (fa); Tay-sachs (zh); ტეა-საქსის სინდრომი (ka); Tay-sachs (zh-hk); Tayov-Sachsov syndróm (sk); טאי זקס (he); Тей-Сакс чире (tt); Tay-sachs (zh-hant); Tay–Sachsin tauti (fi); malsano de Tay-Sachs (eo); Tay-Sachsova choroba (cs); Tay-Sachsova bolest (bs); malattia di Tay-Sachs (it); maladie de Tay-Sachs (fr); Tay-Sachsi haigus (et); Bệnh Tay–Sachs (vi); テイ=サックス病 (ja); Теј-Саксова болест (sr); Tay-Sachsova bolezen (sl); Tay-sachs (zh-hans); ଟେ-ସାକ୍‌ସ ଡିଜିଜ (or); Թեյ-Սաքսի հիվանդություն (hy); хвороба Тея-Сакса (uk); Choroba Taya-Sachsa (pl); ടേ-സാക്സ് രോഗം (ml); Ziekte van Tay-Sachs (nl); malaltia de Tay-Sachs (ca); Tay-Sachs (ms); Boala Tay-Sachs (ro); Tay-Sachs hastalığı (tr); Tay-Sachs disease (en); داء تاي ساكس (ar); Νόσος Tay-Sachs (el); doença de Tay-Sachs (pt) malattia (it); maladie neurodégénérative (fr); מחלה גנטית (רצסיבית) קטלנית (he); Krankheit (de); afectiune genetica (ro); Human medical condition (en); تای ساکس (fa); κληρονομική νευρολογική διαταραχή (el); vrozená vada nervové soustavy (cs) Idiocia Amaurótica Familiar, Idiocia Amaurotica Familiar, Enfermedad de Tay Sachs, deficiencia de hexosaminidasa A (es); gangliosidose à GM2 variante B, idiotie amaurotique familiale (fr); Болезнь Тея-Сакса (ru); Tay-Sachs-Krankheit, Morbus Tay-Sachs (de); Tay-Sachs (pt); Gangliozidoza MG2 (ro); テイサックス病, TSD, テイ-サックス病, Tay-Sachs病, テイ・サックス症, テイ・サックス病 (ja); Tay-Sachs, Gangliosidióza (sk); Choroba Taya i Sachsa, Idiotyzm rodzinny, Choroba Tay-Sachsa (pl); Тея-Сакса хвороба (uk); Ziekte van Tay Sachs (nl); síndrome de Tay-Sachs, deficiència d'hexosaminidasa A (ca); Tay–Sachs disease, റ്റെയ്-സാക്സ് രോഗം, ടേ-സാക്സ് (ml); Tay-Sachsin tauti (fi); hexosaminidase A deficiency, Tay-Sachs disease (disorder), disease, Tay-Sachs, GM2 gangliosidosis, type 1, Hexosaminidase a Deficiency, Adult Type, Hexosaminidase alpha-subunit deficiency (variant B), Gm2-Gangliosidosis, Variant B1, Gm2-Gangliosidosis, Adult Chronic Type, B variant GM2 gangliosidosis, Gm2-Gangliosidosis, Type 1, Hexa Deficiency, GM2 gangliosidosis, B, B1 variant, Sphingolipidosis, Tay-Sachs, TAY-SACHS DISEASE; TSD, TSD, Tay-Sachs Disease, Variant B1, Tay-Sachs Disease, Juvenile, Tay-Sachs Disease, Pseudo-Ab Variant, B Variant Gm2-Gangliosidosis, TAY-SACHS DISEASE, Gangliosidosis GM2 , type 1 (en); TSD, Tay-Sachs disease (ar); Tay-Sachs, TSD, GM2 gangliozidóza, Tay-Sachsův syndrom, Tay-Sachsova nemoc (cs); מחלת טאי-זקס, מחלת טאי זקס, מחלת טיי-זקס, מחלת טיי זקס, טיי זקס, טיי-זקס, טאי-זקס (he)
Tay-Sachs disease 
Human medical condition
Tay-sachsUMich.jpg
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Instance ofrare disease
Subclass oflysosomal storage disease,
GM2 gangliosidosis,
eye degenerative disease
Named after
Discoverer or inventor
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Subcategories

This category has the following 2 subcategories, out of 2 total.

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